Reported Jul 12, 2023 · Ongoing

KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin…

Pro-Dex Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Pro-Dex Inc · 2361 McGaw Ave · Irvine, CA · 92614-5831

Is this the product you have?

  • KLS Martin Battery Pack
  • REFKLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver
Lot codes and dates
  • REFKLS-BP-001/KLS-BP-040
  • UDI-DI00862377000140
  • LotK0M6U
  • Expiration8/31/2024
Amount recalled
2000

Where it was sold

Why it was recalled

Battery packs used in surgical procedures where a surgeon uses a powered screwdriver and a right-angle attachment have switched manufacturing and expiration dates on sterile pouch labels, so batteries will appear to be prematurely expired.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:55 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.